A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035128



Internal ID19124347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21196301..21269670hg38UCSC Ensembl
Innerchr9:21196300..21269669hg19UCSC Ensembl
Innerchr9:21186300..21259669hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3873370
hg1973370
hg1873370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755835
Samples
Known GenesIFNA10, IFNA14, IFNA16, IFNA17, IFNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035128
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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